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The standardized absolute risk of an outcome was estimated as the averaged person-specific absolute risk over each cohort under a given treatment modality

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This analysis highlights the ability to rapidly assess early real-world uptake of newly approved therapies within weeks of FDA authorization, enabling timely characterization of initial prescribing patterns as they emerge in clinical practice

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They have shown reasonable accuracy in diagnosing advanced fibrosis and good performance in excluding the majority of patients with a low risk of liver-related complications